• 2022 WHO classification of renal cell carcinomas: Focus on papillary renal cell carcinoma
• A 7-year-old boy presented with temporal lobe lesion
• A Case of SMARCB1-Deficient Sinonasal Carcinoma With Clear Cell Morphology
• A case of surgically treated non-metastatic SMARCA4-deficient undifferentiated thoracic tumor: a case report and literature review
• A kinome drug screen identifies multi-TKI synergies and ERBB2 signaling as a therapeutic vulnerability in MYC/TYR subgroup ATRTs
• A Rare Case of a Malignant Epithelioid Neoplasm With an Underlying Novel <em>EWSR1::ZBT44</em> Fusion, Identified on Next-Generation Sequencing (NGS)
• Aberrant DNA methylation distorts developmental trajectories in atypical teratoid/rhabdoid tumors
• Accuracy of contrast-enhanced CT in liver neoplasms in children under 2 years age
• ALK-Rearranged Renal Cell Carcinoma: A Multi-Institutional Study of 9 Cases With Expanding the Morphologic and Molecular Genetic Spectrum
• ALK-rearranged renal cell carcinoma: a multi-institutional study of nine cases with expanding the morphologic and molecular genetic spectrum
• An adult with recurrent atypical teratoid rhabdoid tumor of the spine
• Angiosarcoma of the head and neck: A clinicopathologic study with special emphasis on diagnostic pitfalls
• Atypical teratoid rhabdoid tumor in a lower middle-income country: Challenges to cure
• Atypical teratoid rhabdoid tumor in a lower middle‑income country: Challenges to cure
• Atypical teratoid/rhabdoid tumor of the central nervous system: Clinicopathological features of two challenging cases
• Atypical teratoid/rhabdoid tumour-TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition
• Autologous stem cell transplantation in adults with atypical teratoid rhabdoid tumor: a case report and review
• Case report: A rare case of omental extrarenal rhabdoid tumor and review of the literature
• Case report: Gastric carcinoma with SMARCA4 deficient: two cases report and literature review
• Case report: Salivary duct carcinoma in a patient with a germline <em>CDH1</em> pathogenic variant - expanding the spectrum of hereditary cancer predisposition syndromes
• Central nervous system embryonal tumors with EWSR1-PLAGL1 rearrangements reclassified as INI-1 deficient tumors at relapse
• Cerebrospinal fluid cytology in a case of epithelioid glioblastoma
• Clinical and histopathological spectrum of cranial small round cell tumors: An experience from a tertiary care center
• Clinical protocol phase II study of tumor infiltrating lymphocytes in advanced tumors with alterations in the SWI/SNF complex: the TILTS study
• Clinical T1/2 renal cell carcinoma: multiparametric dynamic contrast-enhanced MRI features-based model for the prediction of individual adverse pathology
• Clinicopathological features of BAP1 mutated clear cell renal cell carcinoma
• Clinicopathological features of two ultra-rare cases of malignant perivascular epithelioid cell tumors (PEComas) involving the uterus with recent updates
• Congenital Disseminated Malignant Rhabdoid Tumor Mimicking a Vascular Lesion
• Cytokine Signaling in Pediatric Kidney Tumor Cell Lines WT-CLS1, WT-3ab and G-401
• Cytomorphology of metastatic colonic MXD4::NUTM1-rearranged sarcoma
• Detection of tumor-derived cell-free DNA in cerebrospinal fluid using a clinically validated targeted sequencing panel for pediatric brain tumors
• Diffuse infiltrating tumour with the molecular profile of an atypical teratoid rhabdoid tumour (AT/RT SHH-1B) in an adult patient
• Discovery of CW-3308 as a Potent, Selective, and Orally Efficacious PROTAC Degrader of BRD9
• Dynamic Survival Risk Prognostic Model and Genomic Landscape for Atypical Teratoid/Rhabdoid Tumors: A Population-Based, Real-World Study
• Effect of emergent nephrostomy on long-term total and split renal function in patients with upper urinary tract obstruction due to pelvic malignant tumors
• Elusive and Aggressive: Unraveling SMARCB1/INI1-Deficient Undifferentiated Carcinoma With Rhabdoid Features Arising From the Colon: A Case Report and Comprehensive Literature Review
• Epidemiology, Characteristics and Prognostic Factors of Primary Atypical Teratoid/Rhabdoid Tumours in the Spinal Canal: A Systematic Review
• Epidemiology, treatment and outcomes of primary renal sarcomas in adult patients
• Epigenetic age acceleration is a distinctive trait of epithelioid sarcoma with potential therapeutic implications
• Epigenetic targeting of PGBD5-dependent DNA damage in SMARCB1-deficient sarcomas
• Esophageal carcinoma with <em>SMARCA4</em> mutation: a narrative review for this rare entity
• ESTRO-SIOPE guideline: Clinical management of radiotherapy in atypical teratoid/rhabdoid tumors (AT/RTs)
• Expanding the Spectrum of NUTM1 -Rearranged Sarcoma : A Clinicopathologic and Molecular Genetic Study of 8 Cases
• Expanding the Spectrum of NUTM1-Rearranged Sarcoma: A Clinicopathologic and Molecular Genetic Study of 8 Cases
• False-Positive Asymmetrical Tongue Muscle 18F-FDG Uptake in Hypoglossal Nerve Paralysis Following Lymph Node Dissection in a Pediatric Patient with Malignant Rhabdoid Tumor of the Neck
• Feeder-free differentiation of human iPSCs into natural killer cells with cytotoxic potential against malignant brain rhabdoid tumor cells
• FNA of Meningioma with Rhabdoid Features Presenting as a Lateral Neck Mass
• Gastric SMARCA4-deficient undifferentiated tumor (SMARCA4-UT): a clinicopathological analysis of four rare cases
• High-Grade Atypical Teratoid/Rhabdoid Tumor in the Pituitary Region
• How to improve initial diagnostic accuracy of kidney tumours in childhood?-A non-invasive approach
• Imaging of supratentorial intraventricular masses in children:a pictorial review- part 1
• Imaging performance of thoracic SMARCA4-deficient undifferentiated tumor: a case report and literature review
• Infiltrating lobular carcinoma of LUMB HER2+ subtype with rhabdoid feature coexisting with synchronous malignant transformation of phyllodes tumor: An exceedingly rare clinicopathological characteristic in Vietnam
• Knocking out CD70 rescues CD70-specific nanoCAR T cells from antigen-induced exhaustion
• Late-onset tumors in rhabdoid tumor predisposition syndrome type-1 (RTPS1) and implications for surveillance
• Malignant Extrarenal Rhabdoid tumor derived from the greater omentum: A case report and literature review
• Malignant Rhabdoid Tumor and Related Pediatric Tumors: Multimodality Imaging Review with Pathologic Correlation
• Malignant rhabdoid tumor of the orbit in an infant
• Malignant rhabdoid tumor of the urinary bladder in a 1-year and 9-month-old girl: A case report and literature review
• Marked Response to Nivolumab by a Patient With SMARCA4-Deficient Undifferentiated Urothelial Carcinoma Showing High PD-L1 Expression: A Case Report
• Mediastinal malignant rhabdoid tumor in an infant: A rare case report
• Mesenchymal neoplasms of the tongue: A clinicopathologic study of 93 cases
• Multifocal intraosseous pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma: A rare presentation of an uncommon tumor
• Multiple primary tumors in children: a clinicopathological analysis of four cases
• Neonatal rhabdoid tumor presenting as feeding intolerance and vomiting: A case report
• NRP1 knockdown inhibits the invasion and migration of rhabdoid tumor of the kidney cells
• Outcomes for children with recurrent/refractory atypical teratoid rhabdoid tumor: A single-institution study with molecular correlation
• Paired Primary and Recurrent Rhabdoid Meningiomas: Cytogenetic Alterations, BAP1 Gene Expression Profile and Patient Outcome
• Pathological Diagnosis and Genetic Alterations of Meningioma
• Pediatric atypical teratoid/rhabdoid tumor in the cauda equina with rapid tumor progression: illustrative case
• Plasma miRNA expression profile in pediatric pineal pure germinomas
• Post-zygotic mosaicism of SMARCB1 variants in patients with rhabdoid tumors: a not so rare condition exposing to successive tumors
• Rare Coexistence: Pilocytic Astrocytoma With Atypical Teratoid/Rhabdoid Tumor Features in an Infant
• Recurrence Patterns and Surveillance Imaging in Pediatric Brain Tumor Survivors
• Renal cell carcinoma preceded by a rheumatoid‑like paraneoplastic syndrome: A case report
• Renal synovialosarcoma: What about pyelic cytology to make a diagnosis?
• Resection of a primary mediastinal malignant rhabdoid tumor: A study in multidisciplinary collaboration and 3-dimensional printing
• Retrospective experience of children with relapsed brain tumors treated with oral combination of axitinib and metronomic etoposide
• Rhabdoid tumor predisposition syndrome: A historical review of treatments and outcomes for associated pediatric malignancies
• Role of Interleukin 1 Receptor 2 in Kidney Disease
• SMARCA4-deficient primary bone sarcoma with "teratoid" features in a rhabdoid tumor predisposition syndrome patient
• SMARCB1 Gene Therapy Using a Novel Tumor-Targeted Nanomedicine Enhances Anti-Cancer Efficacy in a Mouse Model of Atypical Teratoid Rhabdoid Tumors
• SMARCB1/INI1-deficient undifferentiated carcinoma of the ileum with features of rhabdoid tumor: A case report
• Spinal Atypical Teratoid Rhabdoid Tumor in a 14-Year-old Child With Down Syndrome: A Case Report
• Subungual melanoma with cartilaginous differentiation: Molecular insights
• Super-Enhancer Dysregulation in Rhabdoid Tumor Cells Is Regulated by the SWI/SNF ATPase BRG1
• Survivors of infant atypical teratoid/rhabdoid tumors present with severely impaired cognitive functions especially for fluid intelligence and visual processing: data from the German brain tumor studies
• SWI/SNF Complex-Deficient Undifferentiated Carcinoma of the Pancreas: Clinicopathologic and Genomic Analysis
• SWI/SNF COMPLEX-DEFICIENT UNDIFFERENTIATED CARCINOMA OF THE PANCREAS:CLINICOPATHOLOGIC AND GENOMIC ANALYSIS
• Synergistic Antitumor Activity of Talazoparib and Temozolomide in Malignant Rhabdoid Tumors
• Targeting cholesterol biosynthesis for AT/RT: comprehensive expression analysis and validation in newly established AT/RT cell line
• Targeting dependency on a paralog pair of CBP/p300 against de-repression of KREMEN2 in SMARCB1-deficient cancers
• The heterogeneous sensitivity of pediatric brain tumors to different oncolytic viruses is predicted by unique gene expression profiles
• The prognostic role of histomorphological subtyping in nonmetastatic papillary renal cell carcinoma after curative surgery: is subtype really irrelevant? A propensity score matching analysis of a multi-institutional real life data
• Thoracic SMARCA4-deficient tumors: a clinicopathological analysis of 52 cases with SMARCA4-deficient non-small cell lung cancer and 20 cases with thoracic SMARCA4-deficient undifferentiated tumor
• TROP-2, NECTIN-4 and predictive biomarkers in sarcomatoid and rhabdoid bladder urothelial carcinoma
• Tumoral EIF4EBP1 regulates the crosstalk between tumor-associated macrophages and tumor cells in MRTK
• Two Cases of Atypical Teratoid/Rhabdoid Tumor in the Spinal Cord: Loss of SMARCB1 in a Child and Loss of SMARCA4 in an Adult
• Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors
• Uterine tumors mimicking ovarian sex cord tumors with rhabdoid differentiation: a clinicopathologic study of 4 cases: A case series analysis